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Vaser 110-0037

by Solta Medical, Inc.

Ref 110-0037

Vaser 110-0037 is a device classified as Class IIb in the EU and Class II in the US made by Solta Medical, Inc., registered in EUDAMED on 18 May 2026 (Basic UDI-DI B-00850608002537) and listed in FDA GUDID since 23 Sep 2016 (UDI-DI 00850608002537), active as of 22 Oct 2026.

Active European Union. Also listed in GUDID (US).

CE MDD

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-00850608002537 Basic UDI-DI 00850608002537UDI-DIDate18 May 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00850608002537 UDI-DI Date23 Sep 2016ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-00850608002537 registered 18 May 2026 Active
  • FDA GUDID UDI-DI 00850608002537 listed 23 Sep 2016 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00850608002537
  2. Registered EUDAMED B-00850608002537

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDD Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade name
VASER Pro Amplifier 230VAC EUDAMED
Vaser GUDID
Generic name
Ultrasonic surgical system generator
Model / Ref / Catalog
110-0037
Primary DI / UDI-DI
00850608002537
Basic UDI-DI
B-00850608002537
FDA product code
MUU
EMDN code
Z12040214 Liposuction systems
GMDN term
Ultrasonic surgical system generator
Device class
Class IIb EUDAMED
Class II GUDID
Regulation number
878.5040
EU registration type
Legacy device (under a directive)
EU market of registration
Netherlands
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device classEUDAMED
Class IIb
GUDID
Class II

Device class is stated on each registry's own scale: Class IIb in the EU (EUDAMED), Class II in the US (FDA GUDID). EU and US classes are different schemes, so this is not a disagreement.

Related devices

Category: Ultrasonic surgical system generator

Similar devices in this category

Other devices filed under LIPOSUCTION SYSTEMS.

Other devices from Solta Medical, Inc.

See all devices from Solta Medical, Inc. →

Properties

  • Prescription use
  • Serial number
  • Manufacturing date
Other properties (20, all answered No)